Apolipoprotein E*3-Leiden allele results from a partial gene duplication in exon 4 (Q69403147)

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1 October 2019

title

Apolipoprotein E*3-Leiden allele results from a partial gene duplication in exon 4 (English)

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1 October 2019

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A M van den Maagdenberg

1

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1 October 2019

P de Knijff

2

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1 October 2019

A F Stalenhoef

3

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1 October 2019

J A Gevers Leuven

4

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1 October 2019

L M Havekes

5

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1 October 2019

R R Frants

6

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1 October 2019

language of work or name

English

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publication date

1 December 1989

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Biochemical and Biophysical Research Communications

1 October 2019

published in

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1 October 2019

volume

165

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1 October 2019

issue

2

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1 October 2019

page(s)

851-857

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Polymorphism of apolipoprotein E and occurrence of dysbetalipoproteinaemia in man

1 October 2019

cites work

1 reference

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Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19.

7 January 2021

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Identification of a new structural variant of human apolipoprotein E, E2(Lys146 leads to Gln), in a type III hyperlipoproteinemic subject with the E3/2 phenotype

7 January 2021

1 reference

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Apolipoprotein E2-Christchurch (136 Arg----Ser). New variant of human apolipoprotein E in a patient with type III hyperlipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2889%2980044-0

A novel electrophoretic variant of human apolipoprotein E. Identification and characterization of apolipoprotein E1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2889%2980044-0

Analysis of apolipoprotein E5 gene from a patient with hyperlipoproteinemia

7 January 2021

1 reference

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Analysis of apolipoprotein E7 (apolipoprotein E-Suita) gene from a patient with hyperlipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2889%2980044-0

Apolipoprotein E3-Leiden. A new variant of human apolipoprotein E associated with familial type III hyperlipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2889%2980044-0

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

7 January 2021

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The human thyroglobulin gene contains two 15-17 kb introns near its 3'-end

7 January 2021

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10.1016/S0006-291X(89)80044-0

7 January 2021

Identifiers

DOI

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1 October 2019

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